Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoprene | HCID 6557 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | 1-Ethenyl-4-methylbenzene | HCID 12161 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Isoprene butadiene | HCID 168288 | — |
| Product | Styrene p-methylstyrene | HCID 19702659 | — |
Reaction Steps
In a pressure-tight case equipped with a stirrer, 2700 g of cyclohexane, 70 g of a 40:60 monomer mixture of p-methylstyrene and styrene, and 2.52 ml of 1.3 mol cyclohexane solution of sec-butyllithium were placed and polymerized at 50° C. for 120 minutes. The resulting mixture was further polymerized with 326.6 g of a 60:40 monomer mixture of isoprene and butadiene for 120 minutes, and was further polymerized with 70 g of a 40:60 monomer mixture of p-methylstyrene and styrene for 120 minutes. The polymerization was then terminated by the addition of methanol and thereby yielded a poly(p-methylstyrene/styrene)-poly(isoprene/butadiene)-poly(p-methylstyrene/styrene) triblock copolymer. The triblock copolymer was dissolved in cyclohexane, and the resulting solution was placed in a pressure-tight case, whose atmosphere had been sufficiently replaced with nitrogen gas. The solution was subjected to hydrogenation using a Ni/Al Ziegler hydrogenation catalysis at 80° C. in an atmosphere of hydrogen gas for 5 hours and thereby yielded a poly(p-methylstyrene/styrene)-hydrogenated poly(isoprene/butadiene)-poly(p-methylstyrene/styrene) triblock copolymer [Mn=200000; proportions of polymer blocks=15/70/15 (by weight); hydrogenation ratio of poly(isoprene/butadiene) block=99% by mole] [addition block copolymer (I0-5a)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07074855B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-61df165efc81456c875f291a49f95b22 |
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| Source note | uspto-grants-2006_07 |
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